Volume 22, Issue 12 pp. 2208-2211

Defective triggering of secondary peristalsis in patients with non-erosive reflux disease

Katsuhiko Iwakiri

Corresponding Author

Katsuhiko Iwakiri

Department of Medicine, Division of Gastroenterology, Nippon Medical School, and

Dr Katsuhiko Iwakiri, Department of Medicine, Division of Gastroenterology, Nippon Medical School, Sendagi 1-1-5, Bunkyo-ku, Tokyo 113-8603, Japan. Email: [email protected]Search for more papers by this author
Yoshinori Hayashi

Yoshinori Hayashi

Department of Medicine, Division of Gastroenterology, Nippon Medical School, and

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Makoto Kotoyori

Makoto Kotoyori

Department of Medicine, Division of Gastroenterology, Nippon Medical School, and

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Yuriko Tanaka

Yuriko Tanaka

Department of Medicine, Division of Gastroenterology, Nippon Medical School, and

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Noriyuki Kawami

Noriyuki Kawami

Department of Medicine, Division of Gastroenterology, Nippon Medical School, and

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Hirohito Sano

Hirohito Sano

Department of Medicine, Division of Gastroenterology, Nippon Medical School, and

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Kaiyo Takubo

Kaiyo Takubo

Human Tissue Research Group, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan; and

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Choitsu Sakamoto

Choitsu Sakamoto

Department of Medicine, Division of Gastroenterology, Nippon Medical School, and

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Richard H Holloway

Richard H Holloway

Department of Gastroenterology and Hepatology, Royal Adelaide Hospital, Adelaide, Australia

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First published: 19 November 2007
Citations: 35

Abstract

Background and Aim: The pathophysiology of non-erosive reflux disease is poorly understood. Triggering of secondary peristalsis is impaired in patients with erosive esophagitis but data in patients with non-erosive reflux disease are lacking. The aim of this study was to evaluate the difference in esophageal motility between patients with non-erosive reflux disease and healthy subjects.

Methods: Twenty patients with non-erosive reflux disease, with reflux symptoms occurring more than twice per week, and 20 healthy subjects of comparable age and sex underwent esophageal manometry. Primary peristalsis was tested with 10 swallows of a 5-mL water bolus. Secondary peristalsis was triggered by esophageal distention using a 20-mL air bolus, which was injected rapidly into the mid-esophagus. After 20 s, each stimulus was followed by a dry swallow to clear any residual air and then each stimulus was repeated five times.

Results: Basal lower esophageal sphincter pressure, pressure wave amplitude in the upper, middle and lower esophagus, wave velocity and the rates of successful primary peristalsis were similar in non-erosive reflux disease patients and controls. The rate of triggering of secondary peristalsis in patients with non-erosive reflux disease (median 20%, interquartile range 0–40%) was significantly lower (P < 0.0001) than that in healthy subjects (90%, 70–100%). When secondary peristalsis occurred in patients with non-erosive reflux disease, however, there were no differences in the amplitude and velocity of secondary peristalsis between the groups.

Conclusions: Triggering of secondary peristalsis is defective in non-erosive reflux disease. This could lead to prolongation of the contact time between refluxed gastric acid and esophageal mucosa thereby leading to symptoms.

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